Journals / Annals of Medical Research / 2020 / Cilt: 27 - Sayı: 1

Case series of ectodermal dysplasia and evaluation of oral findings: A literature review

Pages
420–425
Publication Date
2022-10-12
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The oral rehabilitation of the patients’ needs multidisciplinary dental treatment.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Ectodermal dysplasia (ED) is a hereditary disease characterized by anomalies in the structures of ectodermal origin.
📊
Key Findings & Data:Because of nutrition, speech andaesthetical problems due to the lack of teeth 22 patients with ED syndrome referred to faculty dentistry clinic.
💡
Conclusion & Impact:The oral rehabilitation of the patients’ needs multidisciplinary dental treatment.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Ectodermal dysplasia (ED) is a hereditary disease characterized by anomalies in the structures of ectodermal origin. This report aimsto determine the oral features of patients with ED syndrome and to present treatment approaches. Because of nutrition, speech andaesthetical problems due to the lack of teeth 22 patients with ED syndrome referred to faculty dentistry clinic. Facial physiognomywas typical for ED and the facial height was decreased due to the vertical dimension and the delalet exfoliation of primary teeth.Also anodontia, hypodontia, delayed eruption, diffuse enamel hypoplasia, conical tooth structure, talon cusps, microdontia, and,transposition in teeth were seen in patients. In most cases, prosthesis were applied to improve the facial aesthetics, speech and oralfunction due to the common hypodontia. The primary goals of the dental treatment of patients with ED are enhancing aesthetics andimproving masticatory function. The oral rehabilitation of the patients’ needs multidisciplinary dental treatment.

🔖

Cite This Article

KORUYUCU, M., GÜRCAN, A. T., SEYMEN, F., YARDIMCI, S. (2022). Case series of ectodermal dysplasia and evaluation of oral findings: A literature review. Annals of Medical Research, Cilt: 27 - Sayı: 1, 420–425. https://ajindex.com/articles/446535

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (17)

  1. Ramesh K, Vinola D, John B. Hypohidrotic ectodermal dysplasia- Diagnostic aids and a report of 5 cases. J Indian Soc Pedod Prevent Dent 2010;1:47-54
  2. Palit A, Inamadar AC. What syndrome is this? Christ-Siemens- Touraine syndrome (anhidrotic/ hypohidrotic ectodermal dysplasia). Pediatr Dermatol 2006;23:396-8
  3. Cambiaghi S, Restano L, Paakkönen K, et al. Clinical findings in mosaic carriers of hypohidrotic ectodermal dysplasia. Arch Dermatol 2000;136:217-24
  4. Wicomb GM, Stephen LX, Beighton P. Dental implications of tooth-nail dysplasia (Witkop syndrome): a report of an affected family and an approach to dental management. J Clin Pediatr Dent 2004;28:107-12
  5. Başak F, Ölmez H, Özçelik C, et al. Bir olgu nedeniyle anhidrotik ektodermal displazi ve ortodontik-protetik yaklaşım. T Klin Diş Hek Bil 1997;3:99-103
  6. Itthagarun A, King NM. Ectodermal dysplasia: A review and case report: Quintessence Int 1997;28:595-602
  7. Franchi L, Branchi R, Tollaro I. Craniofacial changes following early prosthetic treatment in a case of hypohidrotic ectodermal dysplasia with complete anodontia. ASDC J Dent Child 1998;65:116-20
  8. Çokpekin F, Uzel İ. Ektodermal displazi olgusu. AÜ Diş Hek Fak Derg 1982;9:191-8
  9. Queiroz KT, Novaes TF, Imparato JCP, et al. The role of the dentist in the diagnosis of ectodermal dysplasia. RGO, Rev. Gaúch. Odontol. 2017;65:161-7
  10. Kearns G, Sharma A, Perrott D, et al. Placement of endosseous implants in children and adolescents with hereditary ectodermal dysplasia. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1999;88:5-10
  11. Itin PH, Fistarol SK. Ectodermal Dysplasias. American Journal of Medical Genetics Part C (Semin. Med. Genet.) 2004;131:45-51
  12. Huang PY, Driscoll CF. From childhood to adulthood: oral rehabilitation of a patient with ectodermal dysplasia. J Prosthet Dent 2014;112:439-43
  13. Wynbrandt J, Ludman MD. The encyclopedia of genetic disorders and birth defects. New York: Facts On File 1990:110-l
  14. Freire-Maia N. Ectodermal dysplasias--a clinical and genetic study. New York: Alan R, Liss Inc, Pinheiro M, Freire-Maia N. Ectodermal dysplasia: a clinical classification and a causal review. Am J Med Genet 1994;53:153-62
  15. Chen H. Hypohidrotic Ectodermal Dysplasia. In: Atlas of Genetic Diagnosis and Counseling. Springer, New York, NY. 2017;1509-1518
  16. Yavuz I, Baskan Z, Ulku R, et al. Ectodermal dysplasia: Retrospective study of fifteen cases. Arch Med Res 2006;37:403-9
  17. Dhar RS, Bora A. Ectro